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ATP1A2
Genetics of Migraine: Insights Into the Molecular Basis of Migraine Disorders
Supplementary Information for the Skeletal Muscle Molecular Clock Regulates Sarcomere Length Through Titin Splicing
Supplementary Table 2
Beyond Traditional Morphological Characterization of Lung
Comprehensive Analysis of the Expression of Sodium/Potassium-Atpase Α Subunits and Prognosis of Ovarian Serous Cystadenocarcinoma
Supplementary Information Page
Dynamics of a Protein Interaction Network Associated to the Aggregation of Polyq-Expanded Ataxin-1
Migraine in the Era of Precision Medicine
Kidney V-Atpase-Rich Cell Proteome Database
Clinical and Genetic Overview of Paroxysmal Movement Disorders and Episodic Ataxias
Clinical and Genetic Analysis in Alternating Hemiplegia of Childhood: Ten New Patients from Southern Europe
Clinical Profile of Patients with ATP1A3 Mutations in Alternating
Adipose Gene Expression Profiles Reveal Novel Insights Into the Adaptation of Northern Eurasian Semi-Domestic Reindeer
Clinical Benefit of NMDA Receptor Antagonists in a Patient with ATP1A2 Gene Mutation Keisuke Ueda, Fatema Serajee and Ahm M
Utviklingsavvik V02
Probe Set Name Symbol 1598 G at Growth Arres
SUPPLEMENTARY APPENDIX Exome Sequencing Reveals Heterogeneous Clonal Dynamics in Donor Cell Myeloid Neoplasms After Stem Cell Transplantation
Adipose Gene Expression Profiles Reveal Novel Insights Into the Adaptation of Northern Eurasian Semi-Domestic Reindeer (Rangifer
Top View
A Cluster of Differentially Expressed Signal Transduction Genes Identified by Microarray Analysis in a Rat Genetic Model of Alcoholism
Supplemental Figures 04 12 2017
A Conjoint Analysis of Epilepsy and Migraine Through Network- And-Pathway-Based Method
Proteomic Analysis Identifies Distinct Glomerular Extracellular Matrix In
Alternating Hemiplegia of Childhood
Higher Burden of Rare Frameshift Indels in Genes Related to Synaptic
Genomic Profiling of Primary Histiocytic Sarcoma Reveals Two Molecular
Comparative in Silico Analysis of Atp1a3 Gene in Mammals
The Ion Channels and Transporters Gene Expression Profile Indicates A
Pathway Analysis of Commonly Expressed Genes Found in Humans and in Non-Human Primates During Naïve State O Keggid Kegg Namesig
Proteins Identified by Proteomics
S-Nitrosylation in Organs of Mice Exposed to Low Or High Doses of Γ-Rays
Proteomic Landscape of the Human Choroid–Retinal Pigment Epithelial Complex
Early Role for a Na+,K+-Atpase (ATP1A3) in Brain Development
Recurrent De Novo Single Point Mutation on the Gene Encoding Na+/K+
4 353 Skin Oral 1 B
Protein Names IGLC7 A0M8Q6 4 1 55,7 11,3
Changes in the Adult Glun2b Associated Proteome Following Adolescent Intermittent Ethanol Exposure
Rapid-Onset Dystonia-Parkinsonism Phenotype Consistency for a Novel Variant of ATP1A3 in Patients Across 3 Global Populations
Neuronal Modeling of Alternating Hemiplegia of Childhood Reveals Transcriptional Compensation And
Two De Novo Mutations in the Na,K-Atpase Gene ATP1A2 Associated with Pure Familial Hemiplegic Migraine
Downregulation of Exosomal Mir-192-5P and Mir-204-5P In
Of the Differential Expression of Cardiac Muscle Contraction (CMC)
Advances in Genetics of Migraine Heidi G
Complement Activation in Peritoneal Dialysis–Induced Arteriolopathy
Altered Skeletal Muscle Mitochondrial Proteome As the Basis of Disruption of Mitochondrial Function in Diabetic Mice Piotr Zabie
Genetic and Genomic Analysis of Atp1a2 and Its Role in Alcohol
Na+/K+-Atpase Revisited: on Its Mechanism of Action, Role in Cancer, and Activity Modulation
Pulmonary Arterial Hypertension in Familial Hemiplegic Migraine with ATP1A2 Channelopathy
Perkinelmer Genomics to Request the Saliva Swab Collection Kit for Patients That Cannot Provide a Blood Sample As Whole Blood Is the Preferred Sample
Familial Hemiplegic Migraine: a New Gene in an Italian Family
STAT Autism and Intellectual Disability Panel
Early Treatment in Acute Severe Encephalopathy Caused by ATP1A2 Mutation of Familial Hemiplegic Migraine Type 2: Case Report and Literature Review
Probe Set ID Gene Symbol* Gene Name* Change St Error 1393245 AT
Supplementary Table 1: Calcineurin-Sensitive Genes
Role for the Na+/K+ Atpase Pump Alpha 3 (ATP1A3) Subunit in Folding
Tauopathy in the Appswe/PS1ΔE9 Mouse Model of Familial Alzheimer's Disease
Systems Biology Comprehensive Analysis on Breast Cancer For
Structures of P-Type Transporting Atpasesand
Calorie Restriction Prevents Metabolic Ageing Caused by Abnormal SIRT1 Function in Adipose Tissues Cheng Xu , Yu Cai , Pengchen
ATP1A2-Specific Polyclonal Antibody Catalog Number:55179-1-AP Featured Product 1 Publications
ATP1A2 Gene Atpase Na+/K+ Transporting Subunit Alpha 2
In Vivo Mapping of a GPCR Interactome Using Knockin Mice
Ulk4 Regulates Gabaergic Signaling and Anxiety-Related Behavior
Genomic Unity® Neurology Analysis
Familial Hemiplegic Migraine with an ATP1A4 Mutation: Clinical Spectrum and Carbamazepine Efficacy
Genetic Effects of ATP1A2 in Familial Hemiplegic Migraine Type II and Animal Models Stephanie M Gritz1* and Richard a Radcliffe1,2
The Interplay Between Retinal Pathways of Cholesterol Output and Its Effects on Mouse Retina